• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name negative pressure wound therapy powered suction pump
510(k) Number K110647
Device Name RENASYS FOAM NPWT WOUND DRESSING KITS WITH SUCTION PAD; RENASYS GAUZE NPWT WOUND DRESSING KITS WITH SUCTION PAD; RENASYS
Applicant
SMITH & NEPHEW, INC.
970 LAKE CARILLON DR.
ST. PETERSBURG,  FL  33716
Applicant Contact LAURA REYNOLDS
Correspondent
SMITH & NEPHEW, INC.
970 LAKE CARILLON DR.
ST. PETERSBURG,  FL  33716
Correspondent Contact LAURA REYNOLDS
Regulation Number878.4780
Classification Product Code
OMP  
Subsequent Product Code
BTA  
Date Received03/07/2011
Decision Date 06/22/2011
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
-
-